Raw gel electrophoresis of RT-PCR amplicons of a local FMDV strain from clinically diseased cattle using serotype A specific primers.</p
<p>The presence of FMDV RNA was determined using qRT-PCR assays, the serotype was determined from se...
The study aimed for the detection and serotyping of Foot and Mouth Disease virus (FMDV) circulating ...
<p>Oligonucleotide primers and PCR conditions for <i>M. bovis</i> (IV isolate) genes.</p
Lane M: High molecular weight nucleic acid marker (100 bp); lanes S1-S7, tested samples which are ep...
Real time reverse transcriptase polymerase chain reaction on clinical samples from affected cattle t...
FMDV can be shed with milk of infected animals and infect susceptible animals. The possibility of us...
Primers used in real-time RT-PCR of 3D gene, one-step RT-PCR and sequencing reaction of 1D gene of F...
<p>Panel A. Quantitation of FMDV RNA by real-time RT-PCR following isolation by manual (Qiagen) or r...
PCR was carried out as a diagnosis of biological and pathological material from cattle, from 17 farm...
<p>A reverse-transcription polymerase chain reaction (RT-PCR) was developed to differentiate t...
<p>Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expected ...
Lanes M: Gene Ruler 100 bp (ThermoFischer Scientific, Johannesburg, South Africa); lanes 1–5: B. abo...
International audienceIn the context of infectious bovine rhinotracheitis (IBR) control programmes u...
A primer pair was designed from the published nucleotide sequence of the coding region of the bovine...
peer reviewedIn the context of infectious bovine rhinotracheitis (IBR) control programmes using glyc...
<p>The presence of FMDV RNA was determined using qRT-PCR assays, the serotype was determined from se...
The study aimed for the detection and serotyping of Foot and Mouth Disease virus (FMDV) circulating ...
<p>Oligonucleotide primers and PCR conditions for <i>M. bovis</i> (IV isolate) genes.</p
Lane M: High molecular weight nucleic acid marker (100 bp); lanes S1-S7, tested samples which are ep...
Real time reverse transcriptase polymerase chain reaction on clinical samples from affected cattle t...
FMDV can be shed with milk of infected animals and infect susceptible animals. The possibility of us...
Primers used in real-time RT-PCR of 3D gene, one-step RT-PCR and sequencing reaction of 1D gene of F...
<p>Panel A. Quantitation of FMDV RNA by real-time RT-PCR following isolation by manual (Qiagen) or r...
PCR was carried out as a diagnosis of biological and pathological material from cattle, from 17 farm...
<p>A reverse-transcription polymerase chain reaction (RT-PCR) was developed to differentiate t...
<p>Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expected ...
Lanes M: Gene Ruler 100 bp (ThermoFischer Scientific, Johannesburg, South Africa); lanes 1–5: B. abo...
International audienceIn the context of infectious bovine rhinotracheitis (IBR) control programmes u...
A primer pair was designed from the published nucleotide sequence of the coding region of the bovine...
peer reviewedIn the context of infectious bovine rhinotracheitis (IBR) control programmes using glyc...
<p>The presence of FMDV RNA was determined using qRT-PCR assays, the serotype was determined from se...
The study aimed for the detection and serotyping of Foot and Mouth Disease virus (FMDV) circulating ...
<p>Oligonucleotide primers and PCR conditions for <i>M. bovis</i> (IV isolate) genes.</p
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